R. Grocock

发表

Zebrafish MiR-430 Promotes Deadenylation and Clearance of Maternal mRNAs

Anton J. Enright, A. Schier, A. Enright, 2006, Science.

Requirement of bic/microRNA-155 for Normal Immune Function

Anton J. Enright, A. Enright, D. Vetrie, 2007, Science.

Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units

Peter Saffrey, Sean Humphray, Aaron Noll, 2012, Science Translational Medicine.

Variation in the strength of selected codon usage bias among bacteria

P. Sharp, J. Peden, R. Grocock, 2005, Nucleic acids research.

Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns.

Jenny Taylor, Anna Schuh, Adrian Alexa, 2012, Blood.

A comprehensive catalogue of somatic mutations from a human cancer genome

Tom Royce, D. Bentley, L. Chin, 2010, Nature.

The DNA sequence of the human X chromosome

David L. Steffen, R. Durbin, A. Coulson, 2005, Nature.

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

Davis J. McCarthy, Calliope A. Dendrou, Lisa J. Murray, 2015, Nature Genetics.

Synonymous codon usage in Pseudomonas aeruginosa PA01.

P. Sharp, R. Grocock, 2002, Gene.

Genome Sequencing and Analysis of the Tasmanian Devil and Its Transmissible Cancer

Carolyn Tregidgo, Albert J. Vilella, Peter J. Campbell, 2012, Cell.

The DNA sequence and biological annotation of human chromosome 1

I. Dunham, C. Clee, D. R. Bentley, 2006, Nature.

The 100,000 Genomes Pilot on Rare Disease Diagnosis in Healthcare − A Preliminary Report

Julius O. B. Jacobsen, Robert W. Taylor, Eleanor F. Dewhurst, 2021, The New England journal of medicine.

TP53 mutations, tetraploidy and homologous recombination repair defects in early stage high-grade serous ovarian cancer

D. Bentley, R. K. Cheetham, S. Humphray, 2015, Nucleic acids research.

The DNA sequence and biological annotation of human chromosome 1 (vol 441, pg 315, 2006)

R. Durbin, G. McVean, A. Coulson, 2006 .

Whole-genome sequencing of patients with rare diseases in a national health system

Keith W. Muir, William J. Astle, Mark I. McCarthy, 2020, Nature.

An integrated map of genetic variation from 1,092 human genomes

Kenny Q. Ye, Mauricio O. Carneiro, Francisco M. De La Vega, 2012, Nature.

miRBase: microRNA sequences, targets and gene nomenclature

Stijn van Dongen, Anton J. Enright, Sam Griffiths-Jones, 2005, Nucleic Acids Res..

RNA editing of human microRNAs

Anton J. Enright, Richard Wooster, Michael R Stratton, 2006, Genome Biology.

DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage

David C. Schwartz, Jane Loveland, Eric S. Lander, 2006, Nature.

TP 53 mutations , tetraploidy and homologous recombination repair defects in early stage high-grade serous ovarian cancer

Julie, D. Bentley, R. K. Cheetham, 2015 .

Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden

Peter Donnelly, Gil McVean, Paolo Piazza, 2014, Nature Communications.

APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma.

Jason B. Nikas, D. Bentley, R. K. Cheetham, 2013, Cancer research.

DNA sequence and analysis of human chromosome 9

I. Dunham, J. L. Ashurst, D. R. Bentley, 2003, Nature.

The DNA sequence and comparative analysis of human chromosome 10

A. Taylor, J. L. Ashurst, M. C. Jones, 2004, Nature.

The micro RNA target paradigm: a fundamental and polymorphic control layer of cellular expression

James R. Brown, P. Sanseau, M. Barnes, 2007, Expert opinion on biological therapy.

Construction, Visualisation, and Clustering of Transcription Networks from Microarray Expression Data

Stijn van Dongen, Anton J. Enright, Tom C. Freeman, 2007, PLoS Comput. Biol..

Synonymous codon usage in Cryptosporidium parvum: identification of two distinct trends among genes.

P. Sharp, R. Grocock, 2001, International journal for parasitology.

Neonatal Intensive Care Units Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in

Neil A. Miller, E. H. Margulies, J. Weir, 2012 .

Erythrocytosis associated with a novel missense mutation in the BPGM gene

Davis J. McCarthy, Lisa J. Murray, P. Donnelly, 2010, Haematologica.

Whole-genome sequencing of patients with rare diseases in a national health system

William J. Astle, Sri V. V. Deevi, Kenneth G. C. Smith, 2020, Nature.

The DNA sequence and biological annotation of human chromosome 1

I. Dunham, C. Clee, D. R. Bentley, 2006, Nature.

NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

Jimmy D Bell, J. Danesh, G. McVean, 2017, Mucosal Immunology.

APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma.

Jason B. Nikas, D. Bentley, R. K. Cheetham, 2013, Cancer research.